The numbers might make it difficult to get an infusion. I am self-taught and not sure of myself - - but your numbers fall within normal ranges except % sat is a touch low (usually 25-35% of the iron-binding sites on transferrin molecules are filled with iron, meaning the other 65-75% is available to move more iron around ... but what exactly it might mean to be slightly low, I am not sure).
People with WED/RLS are said by WED\RLS specialists to need over 75 or even over 100 ng/ml ferritin, but this information hasn't gotten thru to the labs or general practitioners yet, who say anything over 20 is fine. Ferritin is a tricky one, it's an iron-storage molecule, but its concentration in the blood is not necessarily representative of its concentration in any other body tissue, like the brain. Nevertheless, it tends to be low in the blood when there's a shortage somewhere in the body, and in us, the shortage is more than likely in our brains. It also increases in the blood when there's an infection or chronic systemic inflammation in the body, which might mask the normally low ferritin that would result from low brain iron.
Although the iron consensus guidelines (see in my signature link "The 2018 International RLS Study Group consensus guidelines on IRON TREATMENT for WED/RLS") say anyone under 100 is a candidate, they also state that there is no reason someone with ferritin up to 300 might not benefit. Some doctors, however, won't do it unless your ferritin is below 40. And hematologists who aren't familiar with WED/RLS or willing to learn might refuse you no matter what your ferritin is, with that amount of iron in your blood. I hope you have good luck with this. I had an infusion when my ferritin was high 200's, almost 300, and I benefited nicely from it.
If you want real advice on those numbers, try asking Dr Buchfuhrer, who has graciously for decades given of his own personal time to help people like us. He is a WED/RLS clinical specialist (lots of experience treating us, from simple cases to the most refractory). His email is ...hmmm I see it has been changed to
somno5586@outlook.com. You can see emails and answers that he posts at the website of the Southern California RLS Support Group, which he is affiliated with. Go to rlshelp.org and scroll down to "RLS PATIENT LETTERS AND MEDICAL REPLIES SECTION".
(Don't be turned off by the Important!! note, I guess he just got tied of emails sloppily written on phones)
Take his reply with you to the appointment.